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剖析20S蛋白酶体的组装途径。

Dissecting the assembly pathway of the 20S proteasome.

作者信息

Zühl F, Seemüller E, Golbik R, Baumeister W

机构信息

Max-Planck-Institute for Biochemistry, Martinsried, Germany.

出版信息

FEBS Lett. 1997 Nov 24;418(1-2):189-94. doi: 10.1016/s0014-5793(97)01370-7.

Abstract

Proteasomes reach their mature active state via a complex cascade of folding, assembly and processing events. The Rhodococcus proteasome offers a means to dissect the assembly pathway and to characterize intermediates; its four subunits (alpha1, alpha2, beta1, beta2) assemble efficiently in vitro with any combination of alpha and beta. Assembly studies with wild-type and N-terminally truncated beta-subunits in conjunction with refolding studies allowed to define the role of the propeptide which is two-fold: It supports the initial folding of the beta-subunits and it promotes the maturation of the holoproteasomes.

摘要

蛋白酶体通过一系列复杂的折叠、组装和加工事件达到其成熟的活性状态。红球菌蛋白酶体为剖析组装途径和表征中间体提供了一种手段;它的四个亚基(α1、α2、β1、β2)可以在体外与α和β的任何组合高效组装。对野生型和N端截短的β亚基进行组装研究,并结合重折叠研究,得以确定前肽的作用,该作用具有双重性:它支持β亚基的初始折叠,并促进全蛋白酶体的成熟。

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